Biochemistry tests in Dubai & UAE

Compare available Biochemistry tests, their listed prices and the information provided for each option. Test selection and preparation should be discussed with your clinician.

Tests in this category

1,113

Listed price range

450.00–30,000.00 AED

Clinical preparation

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Biochemistry test prices

Showing 931–945 of 1,113 matching tests.

Biochemistry diagnostic tests, details, and listed prices
Test and description	Specimen	Typical duration	Price	Options
TEST-4545 SLC39A13 Gene Spondylocheirodysplasia, Ehlers-Danlos Syndrome‑like Genetic Test This test detects pathogenic variants in the SLC39A13 gene associated with Spondylocheirodysplasia and Ehlers-Danlos syndrome-like conditions.	Peripheral Whole Blood (EDTA Tube or FTA Card)	3 – 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC39A13 gene"] Parameters [] Preparation ["No specific fasting required"] Indications ["Suspected Spondylocheirodysplasia", "Suspected Ehlers-Danlos syndrome-like presentation", "Family history of related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: Q79.6 Clinical summary This test detects pathogenic variants in the SLC39A13 gene associated with Spondylocheirodysplasia and Ehlers-Danlos syndrome-like conditions.
TEST-5464 SLC45A2 Gene Test This test identifies pathogenic variants in the SLC45A2 gene, which are responsible for Oculocutaneous Albinism Type 4, a rare autosomal recessive disorder affecting melanin produc...	Whole Blood (EDTA), FTA Card, or Extracted DNA	3 to 4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC45A2 gene", "Point mutations", "Small insertions/deletions", "Copy number variations (CNVs)"] Parameters [{"name": "Diagnostic Sensitivity", "reference_range": "99.9%"}, {"name": "Methodology", "reference_range": "Next Generation Sequencing (NGS)"}, {"name": "Gene Coverage", "reference_range": "Full coding region with CNV detection"}] Preparation ["No fasting required", "Inform collection team if on anticoagulants", "Mandatory pre-test genetic counseling session"] Indications ["Diagnosis of Oculocutaneous Albinism Type 4 (OCA4)", "Carrier screening for individuals with family history", "Family cascade testing"] Measurement technique Confirm with laboratory Codes LOINC: 81226-7 ICD-10: E70.329, E70.3, E70.30, Z15.89 Clinical summary This test identifies pathogenic variants in the SLC45A2 gene, which are responsible for Oculocutaneous Albinism Type 4, a rare autosomal recessive disorder affecting melanin production.
TEST-3592 SLC4A11 Gene Corneal Endothelial Dystrophy Type 2 Genetic Test This genetic test analyzes the SLC4A11 gene to detect mutations associated with corneal endothelial dystrophy type 2.	Whole blood (EDTA), buccal swab, extracted DNA, or FTA card	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC4A11 gene", "Point mutations", "Small insertions/deletions", "Copy number changes"] Parameters [] Preparation ["No fasting required", "Share complete clinical history and current medication list"] Indications ["Diagnosis of corneal endothelial dystrophy type 2", "Carrier screening", "Family risk assessment"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: H18.59 Clinical summary This genetic test analyzes the SLC4A11 gene to detect mutations associated with corneal endothelial dystrophy type 2.
TEST-3532 SLC4A4 Gene Renal Tubular Acidosis, Proximal, with Ocular Abnormalities Genetic Test This genetic test identifies mutations in the SLC4A4 gene associated with proximal renal tubular acidosis type II and associated ocular abnormalities.	Whole Blood (EDTA), Extracted DNA (≥1 µg), or FTA Card	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLC4A4 gene coding regions", "SLC4A4 gene splice sites"] Parameters [] Preparation ["Genetic counselling session required prior to sample collection", "Clinical history documentation required"] Indications ["Patients presenting with growth retardation, hyperchloremic metabolic acidosis, and bilateral band keratopathy or glaucoma", "Family cascade screening for SLC4A4-associated pRTA", "Recurrence risk counselling"] Measurement technique Confirm with laboratory Codes LOINC: 51963-5 ICD-10: N25.89 Clinical summary This genetic test identifies mutations in the SLC4A4 gene associated with proximal renal tubular acidosis type II and associated ocular abnormalities.
TEST-3492 SLC4A5 Gene (Renal Tubular Acidosis) Test This genetic test identifies pathogenic variants in the SLC4A5 gene, which are associated with proximal renal tubular acidosis with ocular abnormalities.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC4A5 gene", "Single nucleotide variants", "Indels", "Splice-site mutations"] Parameters [] Preparation [] Indications ["Unexplained metabolic acidosis", "Family history of renal tubular disorders", "Failure to thrive", "Nephrocalcinosis"] Measurement technique Confirm with laboratory Codes LOINC: 81245-8 ICD-10: E72.09 Clinical summary This genetic test identifies pathogenic variants in the SLC4A5 gene, which are associated with proximal renal tubular acidosis with ocular abnormalities.
TEST-5791 SLC52A2 Gene Brown‑Vialetto‑Van Laere Syndrome Type 2 Genetic Test This genetic test identifies pathogenic variants in the SLC52A2 gene associated with Brown‑Vialetto‑Van Laere syndrome type 2.	Peripheral Whole Blood (EDTA) or Extracted DNA; also FTA card acceptable.	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC52A2 gene", "Full coding region sequencing"] Parameters [] Preparation ["No specific fasting required", "No medication or diet restrictions"] Indications ["Suspected Brown‑Vialetto‑Van Laere syndrome type 2", "Progressive hearing loss with neurological symptoms"] Measurement technique Confirm with laboratory Codes LOINC: 103527-5 ICD-10: G31.89, G60.0 Clinical summary This genetic test identifies pathogenic variants in the SLC52A2 gene associated with Brown‑Vialetto‑Van Laere syndrome type 2.
TEST-6337 SLC5A1 Gene Glucose/Galactose Malabsorption Genetic Test This test identifies pathogenic variants in the SLC5A1 gene, which are the cause of glucose/galactose malabsorption (GGM). It provides a definitive molecular diagnosis for this rar...	Whole Blood, Extracted DNA, or FTA Card	3–4 weeks from sample collection	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC5A1 gene", "Copy Number Variations (CNVs) in the SLC5A1 gene"] Parameters [] Preparation ["No specific fasting required", "Inform lab of any relevant medications"] Indications ["Suspected glucose/galactose malabsorption (GGM)", "Severe neonatal diarrhea unresponsive to standard treatment", "Family history of GGM"] Measurement technique Confirm with laboratory Codes LOINC: 94027-2 ICD-10: E74.39 Clinical summary This test identifies pathogenic variants in the SLC5A1 gene, which are the cause of glucose/galactose malabsorption (GGM). It provides a definitive molecular diagnosis for this rare inherited disorder.
TEST-3471 SLC5A5 Gene Thyroid Dyshormonogenesis Type 1 Genetic Test This genetic test evaluates the SLC5A5 gene for pathogenic variants associated with thyroid dyshormonogenesis type 1, an iodide transport defect.	Peripheral blood (whole blood in EDTA tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC5A5 gene", "Iodide transport defect"] Parameters [] Preparation [] Indications ["Congenital hypothyroidism of unknown etiology", "Low radioiodine uptake"] Measurement technique Confirm with laboratory Codes LOINC: 96728-9 ICD-10: E07.1 Clinical summary This genetic test evaluates the SLC5A5 gene for pathogenic variants associated with thyroid dyshormonogenesis type 1, an iodide transport defect.
TEST-6310 SLC6A19 Gene (Hartnup Disorder) Genetic Test This genetic test evaluates the SLC6A19 gene for pathogenic variants associated with Hartnup disorder.	Peripheral whole blood, extracted DNA, or FTA card sample	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC6A19 gene", "Amino acid transport function"] Parameters [] Preparation ["No specific fasting required", "Do not discontinue prescribed medications without consulting a doctor"] Indications ["Diagnosis of Hartnup disorder", "Identification of carriers", "Family history of Hartnup disorder"] Measurement technique Confirm with laboratory Codes LOINC: 85661-7 ICD-10: E72.0 Clinical summary This genetic test evaluates the SLC6A19 gene for pathogenic variants associated with Hartnup disorder.
TEST-5951 SLC7A5 Gene (Phenylketonuria Modifier) Genetic Test This genetic test evaluates the SLC7A5 gene for variants that modify the severity of phenylketonuria (PKU). It helps guide personalized dietary management strategies for affected i...	Peripheral whole blood (EDTA) or extracted genomic DNA	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLC7A5 gene variants", "Genetic modifiers of PKU severity"] Parameters [] Preparation ["No specific fasting required", "Do not alter prescribed dietary formula or medication"] Indications ["Patients diagnosed with Phenylketonuria (PKU)", "Assessment of PKU severity", "Guidance for dietary management in PKU"] Measurement technique Confirm with laboratory Codes LOINC: 48508-4 ICD-10: E70.0 Clinical summary This genetic test evaluates the SLC7A5 gene for variants that modify the severity of phenylketonuria (PKU). It helps guide personalized dietary management strategies for affected individuals.
TEST-3654 SLC7A7 Gene Lysinuric Protein Intolerance Genetic Test This genetic test evaluates the SLC7A7 gene for pathogenic variants associated with Lysinuric Protein Intolerance (LPI).	Peripheral Whole Blood (EDTA)	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC7A7 gene", "Point mutations", "Small insertions/deletions", "Copy number variations (CNV)"] Parameters [] Preparation ["No fasting required", "Provide details of any previous metabolic investigations", "Mandatory comprehensive clinical history and pedigree charting by a certified genetic counselor before blood collection"] Indications ["Suspected diagnosis of Lysinuric Protein Intolerance (LPI)", "Family screening for carriers of SLC7A7 mutations", "Differential diagnosis of aminoacidurias or mitochondrial hepatopathies"] Measurement technique Confirm with laboratory Codes LOINC: 21636-6 ICD-10: E72.2 Clinical summary This genetic test evaluates the SLC7A7 gene for pathogenic variants associated with Lysinuric Protein Intolerance (LPI).
TEST-4777 SLC9A3R1 Gene Analysis for Nephrolithiasis/Osteoporosis, Hypophosphatemic Type 2 Test This diagnostic test evaluates the SLC9A3R1 gene for pathogenic variants associated with hereditary hypophosphatemic nephrolithiasis, osteoporosis, and renal phosphate wasting.	Peripheral whole blood (EDTA tube, 5 mL)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC9A3R1 gene"] Parameters [] Preparation ["Mandatory genetic counselling session", "No fasting required"] Indications ["Diagnosis of hereditary hypophosphatemic nephrolithiasis", "Diagnosis of hereditary osteoporosis", "Family screening for SLC9A3R1-related disorders"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E83.31, N20.0 Clinical summary This diagnostic test evaluates the SLC9A3R1 gene for pathogenic variants associated with hereditary hypophosphatemic nephrolithiasis, osteoporosis, and renal phosphate wasting.
TEST-3668 SLC9A3R1 Genetic Test (Nephrolithiasis/Osteoporosis, Hypophosphatemic Type 2) This diagnostic test evaluates for pathogenic variants in the SLC9A3R1 gene associated with autosomal recessive nephrolithiasis/osteoporosis, hypophosphatemic type 2.	Peripheral whole blood or extracted DNA (EDTA tube)	3–4 weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["Pathogenic variants in the SLC9A3R1 gene"] Parameters [] Preparation ["No fasting required", "Provide a blood sample (EDTA tube) or previously extracted DNA", "Mandatory genetic counseling session required"] Indications ["Suspected autosomal recessive nephrolithiasis/osteoporosis, hypophosphatemic type 2", "Family history of the condition"] Measurement technique Confirm with laboratory Codes LOINC: 47527-7 ICD-10: E83.39 Clinical summary This diagnostic test evaluates for pathogenic variants in the SLC9A3R1 gene associated with autosomal recessive nephrolithiasis/osteoporosis, hypophosphatemic type 2.
TEST-3749 SLCO1B1 Gene Rotor‑type Hyperbilirubinemia Genetic Test This genetic test identifies pathogenic variants in the SLCO1B1 gene associated with Rotor syndrome.	Whole blood (EDTA), dried blood spot (FTA card), or extracted DNA	3–4 weeks from sample receipt	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLCO1B1 gene variants", "Single nucleotide variants", "Small insertions/deletions"] Parameters [] Preparation [] Indications ["Confirm hereditary Rotor syndrome", "Differentiate from other conjugated hyperbilirubinemias"] Measurement technique Confirm with laboratory Codes LOINC: 81247-9 ICD-10: E80.6 Clinical summary This genetic test identifies pathogenic variants in the SLCO1B1 gene associated with Rotor syndrome.
TEST-3791 SLCO1B3 Gene Hyperbilirubinemia (Rotor Type) Genetic Test This genetic test identifies mutations in the SLCO1B3 gene associated with Rotor syndrome, a hereditary cause of conjugated hyperbilirubinemia.	Peripheral Whole Blood	3–4 Weeks	2,800.00 AED	View
View test specifications and preparation Hide test specifications and preparation What it measures ["SLCO1B3 gene mutations", "SLCO1B1 gene mutations"] Parameters [] Preparation ["No fasting required"] Indications ["Suspected Rotor syndrome", "Unexplained conjugated hyperbilirubinemia", "Family history of Rotor syndrome"] Measurement technique Confirm with laboratory Codes LOINC: 77735-7 ICD-10: E80.6, Z15.89, R17 Clinical summary This genetic test identifies mutations in the SLCO1B3 gene associated with Rotor syndrome, a hereditary cause of conjugated hyperbilirubinemia.

Category overview

Biochemistry: overview

Seeking clarity about your body's essential functions is vital for long-term well-being. At DNA Labs UAE, our Biochemistry services utilize advanced automated analyzers to evaluate enzymes, proteins, and metabolites in your blood. Whether you need routine metabolic panels or specialized biochemical testing in the UAE, these tests provide critical data to guide your physician's medical plan. As a leading diagnostic lab in Dubai and the UAE, we guarantee strict confidentiality and rapid, accurate turnaround times. Take charge of your health today. Explore our biochemistry diagnostics below, schedule a convenient home sample collection, or contact our specialists to book your test.

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Biochemistry tests in Dubai & UAE

Biochemistry test prices

Biochemistry: overview

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